4-[(3-bromobenzoyl)amino]-2-hydroxybenzoic acid CAS 1016804-16-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1016804-16-2
Molecular FormulaC14H10BrNO4
Molecular Weight336.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-[(3-bromobenzoyl)amino]-2-hydroxybenzoic acid CAS 1016804-16-2 chemical structure

Description

As a certified reference material (CRM), 4-[(3-bromobenzoyl)amino]-2-hydroxybenzoic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies 4-[(3-bromobenzoyl)amino]-2-hydroxybenzoic acid (CAS 1016804-16-2), a certified reference material (molecular formula C14H10BrNO4, MW 336.14 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution, 4-[(3-bromobenzoyl)amino]-2-hydroxybenzoic acid is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 336.14 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC14H10BrNO4
Molecular Weight336.14 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing
Nitrogen Atoms1

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